NDC 65862-959 – Divalproex Sodium
Divalproex Sodium 125 mg/1 · Tablet, Delayed Release · Oral
Product NDC65862-959
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090554
- Marketed since
- October 24, 2014
- Listing expires
- December 31, 2027
- Pharmacologic class
- Anti-epileptic Agent; Mood Stabilizer
Active ingredients
- Divalproex Sodium 125 mg/1
Uses, dosage, side effects and warnings for Divalproex Sodium →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 65862-959-01 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-01) | Oct 24, 2014 |
| 65862-959-05 | 500 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-05) | Oct 24, 2014 |
| 65862-959-10 | 10 BLISTER PACK in 1 CARTON (65862-959-10) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK | Oct 24, 2014 |
| 65862-959-71 | 7000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-71) | Oct 24, 2014 |
| 65862-959-99 | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-99) | Oct 24, 2014 |
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